Responsibilities: Electronic document publishing, scheduling and coordination of various document complexities (clinical protocols/amendments, nonclinical reports, SAPS, CSRs, related regulatory documentation, etc.) Support various internal functional groups ensuring the compliant use of eCTD Authoring Templates Primary user of Adobe Acrobat, 3rd-party plugins, eCTD Authoring Templates and related tools as required Ensure tracking and archiving of regulatory filings, correspondence and related information for various regulatory applications.
https://www1.jobdiva.com/candidates/myjobs/openjob_outside.jsp?a=irjdnw4aqkb0a5bhkjucv8p00hyqhk05031z6ahtakm0pgjg8f34dc29wtyqerjr&from=COMP&id=11144090&SearchString=&StatesString=&jobseq=2&rowsperpage=30&divisions=&divisions2=
No comments:
Post a Comment